Geochemistry,mineralogy and tectonic setting of deerite‐bearing meta‐ironstones from the Emo Metamorphics of Papua New Guinea

The geochemistry of two deerite‐bearing meta‐ironstones from the Emo Metamorphics of Papua New Guinea suggests that they were deposited as metalliferous cherts enriched in manganese and iron by hydrothermal exhalative activity in an ocean ridge system. Subsequent blueschist facies metamorphism resulted in the formation of the assemblage deerite‐quartz‐albite‐iron oxides‐alkali amphiboles‐spessar‐tine‐stilpnomelane‐apatite, with calcium‐manganese carbonates in one specimen. Assemblages in associated metabasites suggest P‐T conditions of 7 kb at 320°C, which overlap with the P‐T field defined by one of the meta‐ironstones. Oxygen fugacity was probably an important control in determining variations in mineralogy and mineral chemistry. Preliminary data on the trace element geochemistry of associated metabasites are consistent with an ocean ridge environment for the formation of the meta‐ironstones.     

Spessartine Garnets in a Manganiferous Carbonate Formation from Nsuta, Ghana

Abstract: Manganese carbonate ore beds and host rock manganiferous phyllites at the Nsuta mine, western Ghana, contain well developed garnet crystals. Individual crystals are idioblastic, sometimes porphyroblastic, and homogeneous, and are associated with rhodochrosite (with or without kutnahorite), quartz and muscovite. The conspicuous absence of chlorite in garnet-rich assemblages, and of garnet in chlorite-rich rocks, suggest chemical constraints may have been important in the formation of the two minerals. Gondite bands within carbonate ores are interpreted to have resulted from localised processes in which manganese carbonates, in environments rich in alumino-silicate minerals, may have been completely exhausted during metamorphic reactions.     

The geochemistry of carbonatites and related rocks from two carbonatite complexes,south Nyanza,Kenya

Carbonatites, metasomatised country rocks, and carbonatitic calcite and magnetite have been analysed from two carbonatite complexes, Homa and Wasaki, W. Kenya.The carbonatites are all greatly Ce-earth enriched, contain abundant ‘carbonatitic’ trace elements (Sr, Ba, Nb and REE), and generally low concentrations of Cr, Co, Ni, Pb, Ga, Ge, Sn, Bi, Li and Mo. At both complexes early søvite is rich in Sr, and impoverished in other trace elements relative to the alvikites. The late-intruded melacarbonatites contain the greatest concentrations of Ba, REE, Fe and Mn.It is concluded that the accumulation of these elements in the later carbonatites is mainly due to fractionation of carbonates from carbonatite magma which was initially rich in ‘carbonatitic’ trace elements.     

Late Ordovician island‐arc volcanic rocks,northern Capertee Zone,Lachlan Fold Belt,New South Wales

The Cape Hoskins volcanoes form part of the Quaternary volcanic island arc that extends from Rabaul in the east to the Schouten Islands in the west, and they overlie the northerly dipping New Britain Benioff Zone. The products of the volcanoes range in composition from basalt to rhyolite, and are normative in quartz and hypersthene. They contain phenocrysts of plagioclase and subordinate augite, hypersthene, and in most samples iron‐titanium oxides; some samples also contain olivine or quartz or both, and some pumice contains hornblende and, rarely, biotite.

Chemical analyses of 29 volcanic rocks are presented; 22 were also analysed for 17 minor elements — Rb, Ba, Sr, Pb, Zn, Cu, Zr, Y, Ni, Co, Sc, Cr, V, Ga, B, U, and Th.

Chemically the rocks have many of the characteristics of the ‘island arc tholeiitic series’, but do not show a pronounced relative enrichment in iron and appear to be relatively enriched in Sr. Compared with volcanic rocks from the northern part of the Willaumez Peninsula, they are lower in K (but not Na), Ti, Rb, Ba, Zr, Pb, Th, Ni, and probably also V, Cu, and Zn: these differences are attributed to the greater depth of the Benioff Zone beneath the Willaumez Peninsula. The more basic of the Cape Hoskins rocks are similar in most respects to lavas of comparable composition from Ulawun volcano to the east.     

青藏高原西部喜马拉雅期花岗岩类特征及岩石系列

青藏高原西部喜马拉雅期花岗岩类岩石组合为透辉石正长岩－透辉石花岗岩－黑云母（二长）花岗岩,主要造岩矿物有钾长石、斜长石、石英、黑云母、透辉石和角闪石。岩石化学成分富碱、高钾、Ｋ２Ｏ／Ｎａ２Ｏ比值大,微量元素富集Ｒｂ,Ｓｒ、Ｂａ、Ｔｈ、Ｕ和ＬＲＥＥ,Ｓｒ、Ｎｄ同位素组成具有幔源特征,岩石属于钾玄岩（ｓｈｏｓｈｏｎｉｔｅ）系列。     

Mineral Compositions and Equilibria in the Metamorphosed Iron Formation of the Gagnon Region, Quebec, Canada

Forty-seven specimens of the Wabush Iron Formation were collectedfrom ten outcrop areas. Twenty-five specimens contain the assemblage(1), quartz+clinopyroxene+calcite with or without orthopyroxene,grunerite, magnetite, ankerite, and siderite. Five specimenscontain assemblage (2), quartz+clinopyroxene+actinolite+calcite+magnetite+hematite,and two contain assemblage (3), quartz+orthopyroxene+actinolite+magnetite+hematite.In three specimens of assemblage (1), graphite occurs in theabsence of magnetite; pyrrhotite and pyrite occur separatelyor together in specimens with assemblage (1). Thirty-nine clinopyroxenes, 38 orthopyroxenes, 18 grunerites,7 actinolites, 16 calcites, 1 ankerite, and 1 siderite wereanalyzed for iron, manganese, and calcium by X-ray emissionspectrography. Magnesium contents were estimated by assumingstoichiometric proportions. Minerals occurring with hematite show low Fe/(Fe+Mg) ratios,and those in the other assemblages show higher values with awide range of variation. In orthopyroxene, Fe/(Fe+ Mg) rangesfrom 0·17 (with hematite) to 0·77. Regularity in the distributions of Fe, Mn, and Ca between pairsof coexisting minerals shows that equilibrium was attained inmost of the rocks studied. This regularity is also accomplishedin the distribution of Mn between calcite and coexisting silicatesas well as between the silicates themselves. Small differencesin the distributions of Ca and Fe depend on both outcrop areaand mineral assemblage. Phase rule considerations suggest that the specimens with dolomite-ankeriteor magnesitesiderite do not represent equilibrium assemblages.Variations in orthopyroxene compositions in assemblages withpyrite or pyrrhotite, or both, and magnetite indicate non-equilibrationof sulfides with silicates. The presence of the oxygen buffer,magnetite+hematite, attests to the immobility of oxygen duringmetamorphism. Within each outcrop area, over which the temperature and pressureare assumed to have been uniform, variations in the compositionsof the silicates in the sub-assemblages quartz+ orthopyroxene+gruneriteand quartz+orthopyroxene+clinopyroxene+calcite indicate gradientsof µ_H2O µ_CO2 and respectively. As characterizedby the composition of orthopyroxene, both gradients are relativelylow along strike, and high across strike. The direction of gradientsacross strike is almost without reversals, which is consistentwith intergranular diffusion of H₂O and CO₂. Phase rule restrictionsfor a majority of assemblages are not in accord with the simultaneousimposition of µ_H2O and µ_CO2 gradients on the rocks,nor the formation of an H₂O-CO₂ fluid phase during metamorphism.     

The Effects of Fe3? and Mn3? on Aluminum Silicate Phase Relations in North-Central New Mexico, U.S.A.

Aluminum silicate triple-point occurrences are common in metamorphicrocks of northern New Mexico. The three polymorphs show extensivesolid solution, with Fe and Mn substituting for Al. Mineraltextures, the spatial distribution of phases, and the systematicpartitioning of Fe and Mn indicate that the kyanite-andalusite-sillimaniteassemblages crystallized in equilibrium. The compositions ofminerals in the three-phase assemblage vary across the studyarea, recording regional variations in the pressures and temperaturesof metamorphism. The highest-pressure rocks, exposed at RioMora, contain kyanite at higher elevations and sillimanite atlower elevations. A sub-horizontal isograd separates the twominerals. Kyanite and sillimanite have nearly identical Fe contentwhich varies systematically with X_Fe2O3 in hematite or ilmenite.Andalusite occurs only along a single manganiferous layer, incrystals rich in MnAlSiO₅ and saturated in FeAlSiO₅. Triple-pointassemblages can be found wherever the folded manganiferous layercrosses the unfolded kyanite-sillimanite isograd. The TruchasRange, preserving slightly lower pressures of metamorphism,shows kyanite-andalusite-sillimanite in rocks with titaniferoushematite. Andalusite is enriched in Fe relative to kyanite andsillimanite, but no polymorphs contain Mn. Rocks with lowerX_Fe2O3 in hematite have kyanite and sillimanite without andalusite,whereas rocks with pure hematite contain only andalusite. Theshallowest erosional levels are preserved in the western PicurisRange where the three polymorphs occur as pure minerals in ilmenite-bearingrocks. Hematitic samples contain only andalusite which showsextensive solid solution of both Fe and Mn. The assemblage kyanite-andalusite-sillimanite is not invariant.Iron and manganese both add degrees of freedom. These transitionmetals have stabilized the three-phase assemblage, in apparentchemical equilibrium, across a P-T interval of 500-540 ?C, 3?8-4?6kb in rocks from New Mexico. The saturation level of FeAlSiO5in andalusite does not vary with Mn content but does vary withpressure and temperature. Calculations indicate that a 2-3 kbdecrease in pressure or a 25-50 ?C increase in temperature resultsin a 1 mole per cent increase in X_FeAlSiO5 in iron-saturatedandalusite.     

Stratiform and stratabound tungsten mineralisation in the Broken Hill Block,N.S.W.

The Early‐Middle Proterozoic Broken Hill Block contains three types of W occurrences, which show close stratigraphic control. All three types occur within a relatively narrow stratigraphic interval (the ‘Mine Sequence’ Suite of Stevens et al., 1980) comprising a highly variable group of metamorphosed silicic and mafic volcanics, clastic sediments, and exhalative and chemical sediments containing base metals. The first type includes occurrences of W and base metals in bedded calc‐silicate rocks. In the second type, W occurs in layered to non‐layered calcsilicate rocks associated with amphibolite; these are intimately associated in a narrow stratigraphic interval containing abundant, small, Broken Hill type deposits. The third type comprises stratabound, W‐bearing pegmatites, which have been remobilised from quartz‐feldspar‐biotite gneiss and bedded quartz‐tourmaline rocks. Tungsten has been mined only from the third type and only in small quantities. The three types of tungsten deposits show a close spatial relationship with stratiform and stratabound Pb‐Zn mineralisation, including the Broken Hill type. The Pb‐Zn and W deposits are inferred to be genetically related.     

Aragonite and magnesite in eclogites from the Jæren nappe,SW Norway: disequilibrium in the system CaCO3–MgCO3 and petrological implications

Eclogites from the Jæren nappe in the Caledonian orogenic belt of SW Norway contain aragonite, magnesite and dolomite in quartz‐rich layers. The carbonates comprise composite grains that occur interstitially between phases of the eclogite facies assemblage: garnet + omphacite + zoisite + clinozoisite + quartz + apatite + rutile ± dolomite ± kyanite ± phengite. Pressure and temperature conditions for the main eclogite stage are estimated to be 2.3–2.8 GPa and 585–655 °C. Published ultrahigh pressure (UHP) experiments on CaO‐, MgO‐ and CO₂‐bearing systems have shown that equilibrium assemblages of aragonite and magnesite form as a result of dolomite breakdown at pressures >5 GPa. As a result, recognition of magnesite and aragonite in eclogite facies rocks has been used as an indicator for UHP conditions. However, petrological testing showed that the samples studied here have not experienced such conditions. Aragonite and magnesite show disequilibrium textures that indicate replacement of magnesite by aragonite. This process is inferred to have occurred via a coupled dissolution–precipitation reaction. The formation of aragonite is constrained to eclogite facies conditions, which implies that the studied rocks have experienced metasomatic, reactive fluid flow during their residence at high pressure (HP) conditions. During decompression, the bimineralic carbonate aggregates were overgrown by rims of dolomite, which partially reacted with aragonite to form Mg‐calcite. The well‐preserved carbonate assemblages and textures observed in the studied samples provide a detailed record of the reaction series that affected the rocks during and after their residence at P–T conditions near the coesite stability field. Recognition of the HP mechanism of magnesite replacement by aragonite provides new insight into metasomatic processes that occur in subduction zones and illustrates how fluids facilitate HP carbonate reactions that do not occur in dry systems at otherwise identical physiochemical conditions. This study documents that caution is warranted in interpreting aragonite‐magnesite associations in eclogite facies rocks as evidence for UHP metamorphic conditions.     

High‐temperature gold‐copper extraction with chloride flux in lava tubes of Tolbachik volcano (Kamchatka)

Subvolcanic environments in supra‐subduction zones are renowned for hosting epithermal deposits that often contain electrum and native gold, including bonanza examples. This study examined mineral assemblages and processes occurring in shallow‐crust volcanic settings using recent eruption (2012–2013) of the basaltic Tolbachik volcano in the Kamchatka arc. The Tolbachik eruptive system is characterized by an extensive system of lava tubes. After cessation of magma input, the tubes maintained the flow of hot oxidized gases that episodically interacted with the lava surfaces and sulphate‐chloride precipitates from volcanic gases on these surfaces. The gas‐rock interaction had strong pyrometamorphic effects that resulted in the formation of molten salt, oxidized (tenorite, hematite, Cu‐rich magnesioferrite) and skarn‐like silicate mineral assemblages. By analogy with experimental studies, we propose that a combination of these processes was responsible for extraction of metals from the basaltic wall rocks and deposition of Cu‐, Fe‐ and Cu‐Fe‐oxides and native gold.     

Malayaite and tin‐bearing silicates from a skarn at Doradilla via Bourke,New South Wales

An extensive complex zoned skarn is developed at the contact of a leucoadamellite intrusive at Doradilla, NW New South Wales. The skarn is a disequilibrium assemblage resulting from a progressive sequence of replacement of a carbonate precursor. Early grossular‐clinopyroxene rocks are replaced by andradite with 0.5–3.5 wt.% SnO₂ clinopyroxene and quartz. Later alteration along fractures and bedding planes of the garnet‐clinopyroxene quartz assemblage has produced calcite‐malayaite (CaSn0.95Ti0.05SiO₅) veins. The final replacement stage was the overprinting of the silicate phases by assemblages containing sulphides, cassiterite, magnetite, titanite, fluorite, biotite and chlorite. The tin content of garent increases with increasing andradite component suggesting replacement of Fe³⁺ by Sn⁴⁺. Associated clinopyroxenes contain 0.1% SnO₂. The coexistence of titanite and its tin isomorph malayaite with extremely limited solid solution indicates late stage skarn temperatures of less than 400°C.     

Geological and Geochemical Investigation of Three Ophiolite‐Hosted Manganese Prospects,Southeast of Birjand,South Khorasan,East of Iran

The studied ophiolite‐hosted manganese prospects are located in southeast of Birjand, South Khorasan, in the east of Iran. The manganese ores within the ophiolitic sequence in this region occur as small discrete patches, associated with radiolarian chert and shale. Manganese ores in the host rocks are recognizable as three distinct syngenetic, diagenetic, and epigenetic features. The syngenetic manganese ores occurred as bands associated with light‐red radiolarian chert. The diagenetic Mn ores occurred as lenses accompanied by dark‐red to brown radiolarian chert. The epigenetic Mn ores occurred as veins/veinlets within the green radiolarian shale. The major manganese ore minerals are pyrolusite, braunite, bixbyite, ramsdellite, and romanechite showing replacement, colloidal, and brecciated textures. The high mean values of Mn/Fe (15.32) and Si/Al (15.65), and the low mean concentration values of trace elements, such as Cu (85.9 ppm), Ni (249.9 ppm), and Zn (149 ppm), as well as the high concentration values of Si, Fe, Mn, Ba, Zn, Sr, and As in the studied manganese ores furnished sufficient evidence to postulate that the sea‐floor Mn‐rich hydrothermal exhalatives were chiefly responsible for the ore formation, and the hydrogenous processes had negligible role in generation of the ores. The further geological and geochemical evidence also revealed that the ores deposited on the upper parts of the ophiolitic sequence by submarine exhalatives. The intense hydrothermal activities caused leaching of elements such as Mn, Fe, Si, Ba, As and Sr from the basaltic lavas (spilites). After debouching of the sea‐floor exhalatives, these elements entered the sedimentary basin. The redox conditions were responsible for separation of Fe from Mn.     

西南三江造山带火山岩—构造组合及其意义

岩石构造组合是指表示板块边界或特定的板块内部环境特征的岩石结合。中国西南“三江”造山带的火山岩可划分为五种火山岩－构造组合：洋脊型／准洋脊型组合，岛弧及陆缘弧组合，碰撞型组合，碰撞后组合及陆内拉张型组合。阐述了各种火山岩－构造组合的特点及构造含义。对在造山带火山岩岩石－构造组合分析中经常遇到的一些问题，如“构造岩片”研究方法、地球化学判别图解的使用条件、准洋脊型火山型组合的构造含义、蛇绿岩带－火山弧的成对性、岩浆作用的同步性和滞后性、以及火山岩的深部“探针”作用等问题进行了讨论。     

额济纳旗碧玉岭铜矿田成矿特征及找矿标志

碧玉岭铜矿区产出于塔里木-华北板块与哈萨克斯坦板块缝合带,其形成与中奥陶统幔源基性火山喷发活动间歇期海底热液喷流活动有关。容矿岩石为碧玉岩,属于含铁硅质岩类的典型喷流岩或热水沉积岩,是同生成矿阶段的主要产物。造山期矿质发生活化迁移,在断裂破碎带中再次富集成矿,因此矿体分布受喷流岩带与断裂破碎带双重控制。浸染状-块状硫化物矿化受碧玉岩层位与岩性控制,矿化体受断裂破碎带控制。结合成矿地质特征及矿物元素的组合异常特征,初步认为该区的找矿标志为:基性火山岩-碧玉岩-孔雀石、褐铁矿、石膏-Cu、Zn、Ba异常。     

Petrological significance of manganese carbonate inclusions in spessartine garnet and relation to the stability of spessartine in metamorphosed manganese-rich rocks

Idioblastic spessartine garnet pervasively developed in Mn-rich rocks and impure manganese carbonate ore at the Lower Proterozoic Nsuta manganese deposit, Western Ghana, contains abundant inclusions of micritic and microconcretionary carbonates and, to a lesser extent, quartz. Detailed mineralogical and microprobe studies indicate all the carbonate phases (i.e. carbonate inclusions in garnet, carbonates coexisting with garnet and carbonates not directly in contact with garnet, the latter hereafter referred to as matrix carbonates) lie within the rhodochrosite-kutnahorite solid solution series, i.e. ~Mn_55-80(Ca + Mg)_20-45CO₃ to Ca₄₂(Mn + Mg)₅₈(CO₃)₂. Minor compositional differences occur in the various carbonate phases, but partition of major elements among coexisting phases indicate most carbonate minerals strongly fractionate Ca and Mg over coexisting spessartine. The nature, composition and textural relationship of coexisting minerals and inclusions in porphyroblastic spessartine indicate that the latter formed from metamorphic reactions in which rhodochrosite and/or kutnahorite and quartz were consumed, in part corroborating earlier observations on a rhodochrosite precursor for spessartine. Spessartine formation is thus envisaged to have taken place when the predominantly Mn carbonate-quartz assemblage became unstable in the presence of minor amounts of an unknown aluminous phase. Because all the carbonates appear to be low-temperature phases with no indications of significant recrystallisation or homogenisation, it could be argued that the spessartine + rhodochrosite - kutnahorite - quartz - pyrite assemblage stabilised during very low-grade greenschist facies metamorphism under relatively low but uniform f_O2 conditions. These observations also suggest the stability field of spessartine could extend to relatively lower temperatures than currently envisaged.     

Mineralogy and genesis of the metamorphosed manganese silicate rocks (gondite) of Gowari Wadhona,Madhya Pradesh,India

Manganese silicate rocks, interbanded with manganese oxide orebodies, constitute an important stratigraphic horizon in the Mansar formation of the Sausar Group of Precambrian age in India. The manganese silicate rocks of Gowari Wadhona occupy the westernmost flank of the manganese belt of the Sausar Group. These rocks are constituted of spessartite, calcium-rich rhodonite, quartz, manganoan diopside, blanfordite (manganese bearing member of diopside-acmite series), brown manganese pyroxene (manganese bearing aegirine-augite), winchite (manganese bearing richterite-tremolite), juddite (manganese bearing amphibole with richterite, tremolite, magnesioriebeckite and glaucophane molecules), tirodite (manganese bearing amphibole with richterite, cummingtonite and glaucophane molecules), manganophyllite, alurgite, piedmontite, braunite, hollandite (and other lower oxides of manganese) with minor apatite, plagioclase, calcite, dolomite and microcline. A complete mineralogical account of the manganese-bearing phases has been given in the text. It has been shown that the juxtaposition of manganese silicate rocks with dolomitic marble, regional metamorphism to almandine-amphibolite facies and assimilation of pegmatite veins cutting across the manganese formation, were responsible for the development of these manganese silicate rocks and the unusual chemical composition of some of the constituent minerals. It has been concluded that the manganese silicate rocks of Gowari Wadhona were originally laid down as sediments comprising manganese oxides admixed with clay, silica etc. and were later regionally metamorphosed to almandine-amphibolite facies. All evidences indicate that rhodochrosite was not present in the original sediment and the bulk composition of the sediments was rich in manganese. These rocks agree entirely to the detailed nomenclature of the gondites enunciated by Fermor (1909) and amplified by Roy and Mitra (1964) and Roy (1966).     

Genesis of carbonates from the Parnok ferromanganese deposit,Polar Urals

The Parnok deposit is made up of stratiform lodes of iron (magnetite) and manganese (oxide-carbonate, carbonate, and carbonate-silicate) ores localized among terrigenous-carbonate sediments (black shales) on the western slope of the Polar Urals. The lithological study showed that ore-bearing sediments were accumulated in a calm hydrodynamic setting within a relatively closed seafloor area (trap depressions). Periodic development of anaerobic conditions in the near-bottom seawater was favorable for the accumulation of dispersed organic matter in the terrigenous-carbonate sediments. Carbon required to form calcium carbonates in the ore-bearing sediments was derived from carbon dioxide dissolved in seawater. In the organic-rich sediments, carbonates were formed with the participation of carbon dioxide released by the destruction of organic matter. However, δ¹³C values (from 0.5 to ?4.4‰ PDB) suggest a relatively low fraction of the isotopically light biogenic carbon in the host calcite. The most probable sources of Fe and Mn were hydrothermal seepages at the seafloor. The Eh-pH conditions during stagnation were favorable for the precipitation of Fe and accumulation of Mn in a dissolved state. Transition from the stagnation regime to the concentration of oxygen in near-bottom waters was accompanied by oxidation of the dissolved Mn and its precipitation. Thus, fluctuations in Eh-pH parameters of water led to the differentiation of Fe and Mn. Initially, these elements were likely precipitated as oxides and hydroxides. During the subsequent lithification, Fe and Mn were reduced to form magnetite and rhodochrosite. The texture and structure of rhodochrosite aggregates indicate that manganese carbonates already began to form at the diagenetic stage and were recrystallized during the subsequent lithogenetic stages. Isotope data (δ¹³C from ?8.9 to ?17.1‰ PDB) definitely indicate that the oxidized organic matter of sediment served as the main source of carbon dioxide required to form manganese carbonates. Carbonates from host rocks and manganese ores have principally different carbon isotopic compositions. Unlike carbonates of host rocks, manganese carbonates were formed with an active participation of biogeochemical processes. Further processes of metagenesis (T ≈ 250–300°C, P ≈ 2 kbar) resulted in the transformation of textures, structures, and mineral composition of all rocks of the deposit. In particular, increase in temperature and pressure provided the formation of numerous silicates in manganese ores.     

Pervasive assimilation of carbonate and silicate rocks in the Hortavær igneous complex, north-central Norway

The intrusive complex at Hortavær represents a magma transfer zone in which multiple pulses of gabbroic and dioritic magmas evolved along Fe- and alkali-enrichment trends. Extreme alkali enrichment resulted in nepheline-normative and sparse nepheline-bearing monzodioritic and monzonitic rocks. More evolved monzonitic and syenitic rocks are silica saturated and, in some cases, quartz bearing. Previous and current research recognized an abundance of clinopyroxene and other Ca-rich phases, such as scapolite, grossular-rich garnet, and igneous-textured calcite among the mafic and intermediate rocks. Even the most pyroxene-rich samples contain low Sc concentrations, which suggests early, intense fractionation of clinopyroxene. These features and the alkali enrichment are consistent with assimilation of carbonate-rich host rocks. Carbon isotope ratios of the igneous-textured calcite indicate an origin of the carbon from host rocks rich in calcite, consistent with assimilation. However, low _Nd values (−3.4 to −10.2) and moderate initial ⁸⁷Sr/⁸⁶Sr values (0.7052 to 0.7099) indicate the need for assimilation of quartzofeldspathic rocks as well. Models of combined assimilation and fractional crystallization indicate that assimilation of simple end members, either carbonate or silicate, cannot explain the entire data set. Instead, variable proportions of carbonate and silicate materials were assimilated, with the most pronounced assimilation effects in the mafic rocks. The reasons for variable degrees of assimilation are, as yet, uncertain. It is possible that assimilation of calc-silicate rocks with variable carbonate/silicate proportions resulted in the range of observed compositions. However, the importance of carbonate assimilation in mafic rocks compared to felsic ones suggests that assimilation of carbonates was predominant at high temperature and/or mafic magma compositions and assimilation of silicates was predominant at lower temperature and/or felsic magma compositions. We suggest that the ability of the mafic magma to dissolve higher proportions of carbonate contaminants is the result of the magma's ability to form clinopyroxene as a product of assimilation. In any case, extensive carbonate assimilation was possible because CO₂ escaped from the system.     

Exploration rock geochemistry for Pinnacles-type mineralization at Broken Hill, N.S.W., Australia

Geochemical responses in weathered and oxidized surface metasedimentary rocks associated with stratiform lead-zinc mineralization at Stirling Hill (6 km west of Broken Hill) are compared with the geochemical responses in fresh drill core from an equivalent lithostratigraphic section with stratiform lead-zinc mineralization at the Pinnacles Mine (8 km south of Stirling Hill). Mineralization is interpreted as being volcanic exhalative and it lies within highly metamorphosed (sillimanite grade) rocks of the Willyama Supergroup.Surface rocks were classified into groups by discriminant analysis using drill core data from the Pinnacles Mine as the initial training set. The behaviour of elements in surface rocks varies with the rock group but Zn, Pb, Mn, Fe, and Co are leached from all surface rocks relative to fresh drill core.Nothwithstanding the leaching effects of weathering, common geochemical responses to mineralization have been identified in drill core and surface rocks. Coincident positive anomalies for Zn/Ba and Fe/(Na × Ba) ratios and negative anomalies for Na/(Mn × Ca) ratios uniquely define mineralization in both weathered surface rocks and in fresh drill core.The results demonstrate that the pattern of geochemical responses to Pinnacles-type stratiform volcanic-exhalative mineralization in surface rocks has survived the intensive weathering regime in the Broken Hill region.